Canonical Allele Identifier: PA314856
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205606
ClinVar RCV Id: RCV000187591 RCV000711735 RCV001082409 RCV001124346 RCV002317102 RCV003967474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Val194Ala
CA314855
NM_000156.6:c.581T>C